82619-101-01 : NDC 2026 Code

82619-101-01 : Fenofibrate ( Fenofibrate )

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NDC Code : 82619-101-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "82619-101-01",
    "PackageDescription": "90 TABLET in 1 BOTTLE (82619-101-01) ",
    "NDC11Code": "82619-0101-01",
    "ProductNDC": "82619-101",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230907",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA217732",
    "LabelerName": "Creekwood Pharmaceuticals LLC",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "40",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-10-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20230920",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}